Pharmacys Prescription Vapor Rub

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name
Pharmacys Prescription Vapor Rub
Generic name
MENTHOL
Manufacturer
American Consumer Products Corp
Product type
HUMAN OTC DRUG
SPL set ID
6ef328ff-f5c3-515d-e053-2a91aa0a32d3
SPL ID
2c69c634-e137-1428-e063-6294a90aa8f1
Version
4
Effective date
2025-01-23
Source export date
2026-09-28
Source partition
7
Source file
https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:48:04
Harmonized routes table
Harmonized routes
TOPICAL

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warning Warning: For external use only. Not for internal use. Avoid contact with eyes. Do not put in mouth, nostrils, or on wounds or damaged skin.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.